We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies, revised Privacy Policy and Terms of Service.
You are being directed to ZacksTrade, a division of LBMZ Securities and licensed broker-dealer. ZacksTrade and Zacks.com are separate companies. The web link between the two companies is not a solicitation or offer to invest in a particular security or type of security. ZacksTrade does not endorse or adopt any particular investment strategy, any analyst opinion/rating/report or any approach to evaluating individual securities.
If you wish to go to ZacksTrade, click OK. If you do not, click Cancel.
BELLUS (BLU) Completes Enrollment in Two Mid-Stage Studies
Read MoreHide Full Article
BELLUS Health Inc. recently announced that it has completed patient enrollment in two ongoing mid-stage studies on pipeline candidate, BLU-5937, a highly selective P2X3 antagonist.
The company has completed enrollment in phase IIb SOOTHE study of BLU-5937 in refractory chronic cough and phase IIa BLUEPRINT study in chronic pruritus associated with atopic dermatitis (AD).
Three doses of BLU-5937 (12.5 mg, 50 mg, and 200 mg BID) are being evaluated in the targeted population in the SOOTHE study (n=310), a randomized, double-blind, four-week, parallel arm, placebo-controlled study. A total of 249 participants with a baseline awake cough frequency of ≥25 awake coughs per hour were randomized across four arms (1:1:1:1) evaluating the three active doses of BLU-5937 and placebo in the main study. The primary efficacy endpoint is the placebo-adjusted change in the 24-hour cough frequency from baseline to day 28 collected with a cough recorder. An exploratory group of an additional 61 participants with a baseline awake cough frequency of ≥10 and <25 coughs per hour were randomized across two arms (1:1) evaluating one active dose (200 mg BID) and placebo to further evaluate the effect of BLU-5937 in patients with lower cough frequency.
The BLUEPRINT study (n=142) is a multicenter, randomized, double-blind, placebo-controlled, parallel-design study evaluating the efficacy, safety, and tolerability of BLU-5937 in 142 participants with moderate to severe chronic pruritus associated with mild to moderate AD. Participants were randomized into one of two treatment arms (1:1) and receive either 200 mg BID of BLU-5937 or placebo for a four-week treatment period. The primary efficacy endpoint is the change from the baseline in weekly mean Worst Itch-Numeric Rating Scale (WI-NRS) score at week four.
Top-line results from both these studies are expected in December.
Shares gained 4.98% on the update. Shares of the company have gained 106.5% in the year so far compared with the industry’s 0.7% gain.
Image Source: Zacks Investment Research
Last week, the company announced positive findings from a preplanned administrative interim analysis of the ongoing SOOTHE study. An independent statistical team reported that the predefined stringent probability threshold for clinical efficacy was met for at least one dose of BLU-5937.
The successful development and commercialization of the drug will be a significant boost for the company.
However, competition will be stiff for the company as bigwigs like Merck (MRK - Free Report) and Bayer (BAYRY - Free Report) are also developing P2X3 antagonists for refractory chronic cough.
Regeneron’s earnings estimates have been revised upward by 19.8% for 2021 and 14.2% for 2022 over the past 60 days. The stock has surged 33.9% year to date.
See More Zacks Research for These Tickers
Normally $25 each - click below to receive one report FREE:
Image: Bigstock
BELLUS (BLU) Completes Enrollment in Two Mid-Stage Studies
BELLUS Health Inc. recently announced that it has completed patient enrollment in two ongoing mid-stage studies on pipeline candidate, BLU-5937, a highly selective P2X3 antagonist.
The company has completed enrollment in phase IIb SOOTHE study of BLU-5937 in refractory chronic cough and phase IIa BLUEPRINT study in chronic pruritus associated with atopic dermatitis (AD).
Three doses of BLU-5937 (12.5 mg, 50 mg, and 200 mg BID) are being evaluated in the targeted population in the SOOTHE study (n=310), a randomized, double-blind, four-week, parallel arm, placebo-controlled study. A total of 249 participants with a baseline awake cough frequency of ≥25 awake coughs per hour were randomized across four arms (1:1:1:1) evaluating the three active doses of BLU-5937 and placebo in the main study. The primary efficacy endpoint is the placebo-adjusted change in the 24-hour cough frequency from baseline to day 28 collected with a cough recorder. An exploratory group of an additional 61 participants with a baseline awake cough frequency of ≥10 and <25 coughs per hour were randomized across two arms (1:1) evaluating one active dose (200 mg BID) and placebo to further evaluate the effect of BLU-5937 in patients with lower cough frequency.
The BLUEPRINT study (n=142) is a multicenter, randomized, double-blind, placebo-controlled, parallel-design study evaluating the efficacy, safety, and tolerability of BLU-5937 in 142 participants with moderate to severe chronic pruritus associated with mild to moderate AD. Participants were randomized into one of two treatment arms (1:1) and receive either 200 mg BID of BLU-5937 or placebo for a four-week treatment period. The primary efficacy endpoint is the change from the baseline in weekly mean Worst Itch-Numeric Rating Scale (WI-NRS) score at week four.
Top-line results from both these studies are expected in December.
Shares gained 4.98% on the update. Shares of the company have gained 106.5% in the year so far compared with the industry’s 0.7% gain.
Image Source: Zacks Investment Research
Last week, the company announced positive findings from a preplanned administrative interim analysis of the ongoing SOOTHE study. An independent statistical team reported that the predefined stringent probability threshold for clinical efficacy was met for at least one dose of BLU-5937.
The successful development and commercialization of the drug will be a significant boost for the company.
However, competition will be stiff for the company as bigwigs like Merck (MRK - Free Report) and Bayer (BAYRY - Free Report) are also developing P2X3 antagonists for refractory chronic cough.
BELLUS currently carries a Zacks Rank #3 (Hold). A better-ranked stock in the biotech sector is Regeneron Pharmaceuticals (REGN - Free Report) which sports a Zacks Rank #1 (Strong Buy). You can see the complete list of today’s Zacks #1 Rank stocks here.
Regeneron’s earnings estimates have been revised upward by 19.8% for 2021 and 14.2% for 2022 over the past 60 days. The stock has surged 33.9% year to date.